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Health Tech Startup Jobs in Ohio (NOW HIRING)

Manage projects from initial design through startup, installation, and final handover, ensuring ... You will work extensively with industrial automation technologies, including PLCs, HMIs, and custom ...

Manage projects from initial design through startup, installation, and final handover, ensuring ... You will work extensively with industrial automation technologies, including PLCs, HMIs, and custom ...

GTM Engineer - Data & Analytics

Columbus, OH · On-site

$110K - $132K/yr

OH.io is transforming Columbus into America's startup technology capital, aiming to ignite B2B SaaS ... health, and GTM performance in a way non-technical teammates can act on • Partner with RevOps ...

Service Support Coordinator

Westerville, OH · On-site

$17.25 - $22.75/hr

... startup. We design, manufacture and service the mission-critical infrastructure technologies for ... health, without discrimination as to age, race, color, religion, creed, sex, pregnancy status ...

Showing results 41-60

Health Tech Startup information

What are the key skills and qualifications needed to thrive in a health tech startup?

To thrive in a Health Tech Startup, you need a strong background in healthcare or technology, entrepreneurial drive, and adaptability, often supported by experience in product development or digital health solutions. Familiarity with HIPAA compliance, health data integration platforms, and agile project management tools is valuable. Outstanding communication, resilience, and creative problem-solving are key soft skills for success in a fast-changing, collaborative setting. These skills enable you to innovate and navigate the unique challenges of building impactful health technology products in a dynamic startup environment.

What are some typical challenges faced when working at a health tech startup?

Working at a Health Tech Startup often involves adapting to rapid changes, shifting priorities, and resource constraints while building products that comply with strict healthcare regulations. Team members may wear multiple hats, collaborating closely across engineering, clinical, and business functions to bring solutions to market efficiently. While this environment can be fast-paced and sometimes unpredictable, it also offers opportunities to make a significant impact on healthcare and grow rapidly alongside the company. Employees can expect to learn new skills and take on increasing responsibility as the organization scales.

What is a health tech startup?

A Health Tech Startup job involves working for a company that develops innovative technologies to improve healthcare. Roles can vary widely, from software development and data analysis to product management, regulatory compliance, and business development. Employees in this field often work on digital health solutions, medical devices, telemedicine platforms, or AI-driven healthcare applications. The environment is typically fast-paced and requires adaptability, problem-solving skills, and a passion for improving patient outcomes.

What are popular job titles related to Health Tech Startup jobs in Ohio? For Health Tech Startup jobs in Ohio, the most frequently searched job titles are:
What cities in Ohio are hiring for Health Tech Startup jobs? Cities in Ohio with the most Health Tech Startup job openings:
Infographic showing various Health Tech Startup job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

CQV Specialist - Packaging Equipment

Pinnaql

New Albany, OH • On-site

Full-time

Re-posted 15 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a CQV Specialist - Packaging Equipment who will support commissioning, qualification, and validation activities for packaging equipment and systems in a biotechnology manufacturing environment. The role ensures that packaging lines are installed, tested, and documented in compliance with GMP, FDA, and internal quality requirements while supporting project schedules and startup activities. This is an onsite opportunity in New Albany, OH.

Key Responsibilities

  • Support commissioning, qualification, and validation (CQV) activities for primary and secondary packaging equipment and systems.
  • Develop, review, and execute commissioning and qualification documentation including protocols such as IQ, OQ, and PQ.
  • Verify installation and operational readiness of packaging equipment including labelers, cartoners, serialization systems, inspection systems, and associated utilities.
  • Coordinate activities with engineering, quality assurance, validation, manufacturing, and vendors to ensure proper startup and qualification of packaging lines.
  • Support protocol deviations, discrepancy resolution, and documentation updates as required.
  • Assist with risk assessments, test planning, and validation strategies in accordance with project and regulatory requirements.
  • Ensure compliance with cGMP, FDA regulations, and company validation procedures.
  • Support FAT/SAT activities, startup, and troubleshooting during commissioning phases.
  • Maintain accurate documentation and support turnover packages for validated systems.

Qualifications

  • Bachelors degree in Engineering, Life Sciences, or related technical discipline.
  • 5+ years of experience in CQV, validation, or commissioning within pharmaceutical or biotechnology manufacturing environments.
  • 2+ years of experience qualifying packaging line equipment such as fillers, labelers, cartoners, serialization/aggregation systems, vision inspection systems, and case packers.
  • Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices.
  • Experience writing and executing validation documentation (IQ/OQ/PQ, protocols, reports, discrepancies).
  • Ability to work cross-functionally with engineering, quality, operations, and project management teams.
  • Strong technical writing and documentation skills.
  • Experience supporting equipment startup, FAT/SAT, and commissioning activities in a regulated environment.
  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.